Canonical Allele Identifier: CA2062445033
Gene: MVK HGNC NCBI

Linked Data

dbSNP Id: rs1885685116

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109591587_109591589del , CM000674.2:g.109591587_109591589del GRCh38
NC_000012.11:g.110029392_110029394del , CM000674.1:g.110029392_110029394del GRCh37
NC_000012.10:g.108513775_108513777del NCBI36
NG_007702.1:g.22893_22895del , LRG_156:g.22893_22895del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.42+230_42+232del ENSP00000439134.1:n.42+230_42+232del
ENST00000546277.6:c.885+230_885+232del ENSP00000438153.2:n.885+230_885+232del
ENST00000636529.2:n.524+230_524+232del
ENST00000697195.1:c.*649+230_*649+232del ENSP00000513181.1:n.*649+230_*649+232del
ENST00000697196.1:c.*58+230_*58+232del ENSP00000513182.1:n.*58+230_*58+232del
ENST00000697197.1:n.2914+230_2914+232del
ENST00000228510.8:c.885+230_885+232del MANE Select ENSP00000228510.3:n.885+230_885+232del
ENST00000636529.1:c.510+230_510+232del
ENST00000636996.1:c.733+230_733+232del
ENST00000228510.7:c.885+230_885+232del ENSP00000228510.3:n.885+230_885+232del
ENST00000392727.7:c.729+230_729+232del ENSP00000376487.3:n.729+230_729+232del
ENST00000447878.6:c.*332+230_*332+232del ENSP00000415555.2:n.*332+230_*332+232del
ENST00000537237.5:c.*558+230_*558+232del ENSP00000445382.1:n.*558+230_*558+232del
ENST00000539575.4:c.885+230_885+232del ENSP00000443551.2:n.885+230_885+232del
ENST00000539696.5:c.42+230_42+232del ENSP00000439134.1:n.42+230_42+232del
ENST00000540353.1:n.3118+230_3118+232del
ENST00000625889.2:c.729+230_729+232del ENSP00000486846.1:n.729+230_729+232del
ENST00000629016.2:c.*332+230_*332+232del ENSP00000486804.1:n.*332+230_*332+232del
NM_000431.3:c.885+230_885+232del NP_000422.1:n.885+230_885+232del
NM_001114185.2:c.885+230_885+232del NP_001107657.1:n.885+230_885+232del
NM_001301182.1:c.729+230_729+232del NP_001288111.1:n.729+230_729+232del
XM_011538372.1:c.885+230_885+232del XP_011536674.1:n.885+230_885+232del
XM_017019313.2:c.729+230_729+232del XP_016874802.1:n.729+230_729+232del
XM_017019314.1:c.885+230_885+232del XP_016874803.1:n.885+230_885+232del
XM_024448982.1:c.1115_1117del XP_024304750.1:p.Glu372del
NM_000431.4:c.885+230_885+232del MANE Select NP_000422.1:n.885+230_885+232del
NM_001114185.3:c.885+230_885+232del NP_001107657.1:n.885+230_885+232del
NM_001301182.2:c.729+230_729+232del NP_001288111.1:n.729+230_729+232del